PMA P910061S018
- Device
- SOFLEX & SOFPORT POSTERIOR CHAMBER INTRAOCULAR LENSES
- Applicant
- Bausch & Lomb
- PMA number
- P910061
- Supplement
- S018
- Product code
- HQL
- Decision date
- 2009-07-16
- Classification
- Intraocular Lens
- Generic name
- intraocular lens
- Approval order statement
- CHANGE FROM STERILE WATER TO PROCESSED WATER IN FINAL PRODUCT INSPECTION.
Current openFDA PMA Record#
- Device
- SOFLEX & SOFPORT POSTERIOR CHAMBER INTRAOCULAR LENSES
- Applicant
- Bausch & Lomb
- PMA number
- P910061
- Supplement
- S018
- Product code
- HQL
- Generic name
- intraocular lens
- Decision date
- 2009-07-16
- Decision code
- OK30
- Date received
- 2009-06-09
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- CHANGE FROM STERILE WATER TO PROCESSED WATER IN FINAL PRODUCT INSPECTION.